Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer

<p>Abstract</p> <p>Background</p> <p>The overexpression of eukaryotic translation initiation factor 4E (eIF4E), a key regulator of protein synthesis, is involved in the malignant progression of human breast cancer. This study investigates the relationship between eIF4E...

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Main Authors: Zhou Muxiang, Liu Cong, Wang Guo-Ping, Zhou Sheng
Format: Article
Language:English
Published: BMC 2006-09-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/6/231
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spelling doaj-b1f5440253d646258f1533ed94f1840d2020-11-24T23:35:31ZengBMCBMC Cancer1471-24072006-09-016123110.1186/1471-2407-6-231Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancerZhou MuxiangLiu CongWang Guo-PingZhou Sheng<p>Abstract</p> <p>Background</p> <p>The overexpression of eukaryotic translation initiation factor 4E (eIF4E), a key regulator of protein synthesis, is involved in the malignant progression of human breast cancer. This study investigates the relationship between eIF4E and angiogenesis, as well as their prognostic impact in patients with human breast cancer.</p> <p>Methods</p> <p>Immunohistochemical staining was used to determine protein expression of eIF4E, vascular endothelial growth factor (VEGF), interleukin-8 (IL-8), and CD105 in a set of 122 formalin-fixed, paraffin-embedded primary breast cancer tissues. Expression of eIF4E in positive cells was characterized by cytoplasmic staining. Evaluation of VEGF and IL-8 in the same tissue established the angiogenic profiles, while CD105 was used as an indicator of microvessel density (MVD).</p> <p>Results</p> <p>A significant relationship was found between the level of eIF4E expression and histological grade (<it>P </it>= 0.016). VEGF, IL-8, and MVD were closely related to tumor grade (<it>P </it>= 0.003, <it>P </it>= 0.022, and <it>P </it>< 0.001, respectively) and clinical stage (<it>P </it>= 0.007, <it>P </it>= 0.048, and <it>P </it>< 0.001, respectively). Expression of eIF4E was also significantly correlated with VEGF (<it>P </it>= 0.007), IL-8 (<it>P </it>= 0.007), and MVD (<it>P </it>= 0.006). Patients overexpressing eIF4E had significantly worse overall (<it>P </it>= 0.01) and disease-free survival (<it>P </it>= 0.006). When eIF4E, histological grade, tumor stage, ER, PR, Her-2 status and the levels of VEGF, IL-8, MVD were included in a multivariate Cox regression analysis, eIF4E emerged as an independent prognostic factor for breast cancer (<it>P </it>= 0.001), along with stage (<it>P </it>= 0.005), node status (<it>P </it>= 0.046), and MVD (<it>P </it>= 0.004).</p> <p>Conclusion</p> <p>These results suggest that higher eIF4E expression correlates with both angiogenesis and vascular invasion of cancer cells, and could therefore serve as a useful histological predictor for less favorable outcome in breast cancer patients, as well as represent a potential therapeutic target.</p> http://www.biomedcentral.com/1471-2407/6/231
collection DOAJ
language English
format Article
sources DOAJ
author Zhou Muxiang
Liu Cong
Wang Guo-Ping
Zhou Sheng
spellingShingle Zhou Muxiang
Liu Cong
Wang Guo-Ping
Zhou Sheng
Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
BMC Cancer
author_facet Zhou Muxiang
Liu Cong
Wang Guo-Ping
Zhou Sheng
author_sort Zhou Muxiang
title Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
title_short Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
title_full Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
title_fullStr Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
title_full_unstemmed Eukaryotic Initiation Factor 4E (eIF4E) and angiogenesis: prognostic markers for breast cancer
title_sort eukaryotic initiation factor 4e (eif4e) and angiogenesis: prognostic markers for breast cancer
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2006-09-01
description <p>Abstract</p> <p>Background</p> <p>The overexpression of eukaryotic translation initiation factor 4E (eIF4E), a key regulator of protein synthesis, is involved in the malignant progression of human breast cancer. This study investigates the relationship between eIF4E and angiogenesis, as well as their prognostic impact in patients with human breast cancer.</p> <p>Methods</p> <p>Immunohistochemical staining was used to determine protein expression of eIF4E, vascular endothelial growth factor (VEGF), interleukin-8 (IL-8), and CD105 in a set of 122 formalin-fixed, paraffin-embedded primary breast cancer tissues. Expression of eIF4E in positive cells was characterized by cytoplasmic staining. Evaluation of VEGF and IL-8 in the same tissue established the angiogenic profiles, while CD105 was used as an indicator of microvessel density (MVD).</p> <p>Results</p> <p>A significant relationship was found between the level of eIF4E expression and histological grade (<it>P </it>= 0.016). VEGF, IL-8, and MVD were closely related to tumor grade (<it>P </it>= 0.003, <it>P </it>= 0.022, and <it>P </it>< 0.001, respectively) and clinical stage (<it>P </it>= 0.007, <it>P </it>= 0.048, and <it>P </it>< 0.001, respectively). Expression of eIF4E was also significantly correlated with VEGF (<it>P </it>= 0.007), IL-8 (<it>P </it>= 0.007), and MVD (<it>P </it>= 0.006). Patients overexpressing eIF4E had significantly worse overall (<it>P </it>= 0.01) and disease-free survival (<it>P </it>= 0.006). When eIF4E, histological grade, tumor stage, ER, PR, Her-2 status and the levels of VEGF, IL-8, MVD were included in a multivariate Cox regression analysis, eIF4E emerged as an independent prognostic factor for breast cancer (<it>P </it>= 0.001), along with stage (<it>P </it>= 0.005), node status (<it>P </it>= 0.046), and MVD (<it>P </it>= 0.004).</p> <p>Conclusion</p> <p>These results suggest that higher eIF4E expression correlates with both angiogenesis and vascular invasion of cancer cells, and could therefore serve as a useful histological predictor for less favorable outcome in breast cancer patients, as well as represent a potential therapeutic target.</p>
url http://www.biomedcentral.com/1471-2407/6/231
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